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1.
1.  The transformation of 21-0,N-isopropylidene derivatives of 16,17-epiminopregn-5-ene-2,21-diol-20-one into 20-0,N-isopropylidene derivatives of 16,17-epiminopregn-5-ene-3,20-diol-20-one was discovered, and, based on this, a new variant of the synthesis of 16,17-epiminopregn-5-ene-3,21-diol-20-one-3,21-diacetate was proposed.
2.  A new class of steroids with additional tetrahydrofuran and 1,3 -imidazolidine-2thione rings E and F, respectively, was synthesized.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2392–2398, October, 1988.  相似文献   

2.
Liquid-phase alkylation of p-tert-butylphenol (TBP) and p-cresol by olefins and benzyl chloride in the presence of solid heteropoly acids (HPA) H3PW12O40 and 25% H3PW12O40/SiO2 at 100–150°C provides high yields of mono- and disubstituted products. HPAs are more active than H2SO4, easily separated from the reaction mixture and can be used repeatedly. -- () - () H3PW12O40 25% H3PW12O40/SiO2 100–150°C - - . , H2SO4, - - .  相似文献   

3.
1.  An earlier unknown metabolite ofPseudomonas aeruginosa, strain A197, 2-(n-1-heptenyl)-4-quinolone, was isolated.
2.  The main components of the total mixture of alkaloids produced byPseudomonas aeruginosa strain A197 are 2-n-nonyl-4-quinolone (pseudane-IX), 2-n-heptyl-4-quinolone (pseudane-VII), 2-(n-1-nonenyl)-4-quinolone (1pseudene-IX), and 2-(n-1-heptenyl)-4-quinolone (1-pseudene-VII).
3.  The synthesis of 2-(n-1 -heptenyl)- 4 -quinolones was carried out.
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1.  New organophosphorus complexing agents were synthesized: ethylenediamino-N,N'-diethylphosphonic, N,N-dimethylethylenediamino-N,N-dimethylphosphonic, and N,N-dimethylethylenediamino-N, N-diethylphosphonic acids and also the iodomethylate of the last acid.
2.  The acid dissociation constants for these compounds and the stability constants for their complexes with nickel, copper, dysprosium, and uranyl ions were determined.
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8.
After light irradiation of oil films on water surface the autoxidation process has been found to be of nonsteady auto-oscillatory character, which can be observed in rate oscillations of O2 absorption. Also recorded have been intensity oscillations of the EPR signal from the radical counter added into an oil sample. Complex dynamics of autoxidation can be due to an autocatalytic process involving the participation of peroxides accumulated in oil during photooxidation., , , , O2. , , . , , .  相似文献   

9.
Thermodynamic studies of clathrate hydrates, mainly of structures I and II, are considered in this review which is based on 147 references. There are two main subjects. The first is the host lattice energy and the guest-host interaction energy, both of these quantities being related to the enthalpy of dissociation and composition of the hydrates. The second subject concerns orientational ordering phenomena occurring in both host and guest, as reflected in the low temperature heat capacity. The classical theoretical treatment of clathrate formation has been reconsidered on the basis of recent experimental results. Particular emphasis has been given to orientational ordering since this topic is undoubtedly central to clarifying the nature of clathrate hydrates.Ausgehend von 147 Literaturangaben wurden in diesem Review thermodynamische Untersuchungen von Klathrathydraten hauptsächlich der Struktur I und II betrachtet. Es gibt zwei Hauptaugenmerke. Als erstes die Wirtsgitterenergie und die Gast-Wirt-Wechselwirkungsenergie, beide bezogen auf die Dissoziationsenthalpie und die Bildungsenthalpie der Hydrate. Das zweite Hauptaugenmerk betrifft Orientierungs-Konditionierungserscheinungen sowohl in Wirt als auch Gast, wie in den Wärmekapazitäten bei niedrigen Temperaturen widergespiegelt wird. Auf der Basis jüngster experimenteller Ergebnisse wurde die klassische theoretische Betrachtung über die Bildung von Klathraten überprüft. Der Orientierung-Konditionierung wurde besonderer Nachdruck verliehen, da dies zweifellos eine entscheidende Rolle bei der Klärung der Natur der Klathrathydrate spielt. 147 I II. . «» « — », . «» « », . . , .
Contribution No. 155 from the Chemical Thermodynamics Laboratory.  相似文献   

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1.  The high-resolution13C NMR spectra were analyzed for 16, 17-cyclohexanopregnanes substituted in rings A and B by SR (R=Ph, CH2CH2SH) and S(O)Ph groups. These spectra were used to determine the position of the double bond (4 or 5) and the position and orientation of the 3-SR, 3-SR, 5-SR, and 3-S(O)Ph substituents.
2.  The -, gb-, -, and -effects of the SR (R=Ph, CH2CH2SH) and S(O)Ph substituents on the chemical shifts of the carbon atoms of the steroid skeleton were determined and analyzed. A diastereotopic effect of the S(O)Ph group on the chemical shifts of the carbon atoms of rings A and B was discovered.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1046–1051, May, 1989.  相似文献   

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1.  9-(3-Aminopropyl)adenine, racemic 9-(2-hydroxy-3-amitiopropyl)adenie and its (R)-enantiomer, and 9-(2-hydroxy-3-methylaminopropyl)adenine were synthesized.
2.  A study was made of the NMR spectra of the reaction products of the -tosyloxyalkyl derivatives of uracil and thymine with ammonia and methylamine. Theories were expressed regarding the structure of the formed compounds.
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14.
1.  Liquid cis-1,4-oligodien-1,3-, -glycols have been prepared by the partial ozonolysis of cis-1,4-polydienes-1,3 in inert solvents containing methanol as an active additive in the amount of 1 to 10 moles per 1 mole of ozonide and subsequent reduction of the peroxide ozonolysis products by LiAlH4.
2.  A method is proposed for the determination of the molecular weights of the oligomeric ,-glycols by use of the PMR spectra of their bis(trimethylsilyl) ethers, and the molecular weight distributions of the oligomeric, -glyeols obtained have been established.
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1.  Dienic-dimethylaminocarbonyl compounds were synthesized containing a Br, OEt, or CN substituent in the -position.-Dimethylamino--cyanodienones are found in the open form and do not cyclize to 2H-pyrans.
2.  The existence of a dynamic equilibrium was established between-dimethylamino--bromodienone (or-dimethylamino--ethoxydienone) and 3-bromo-2-dimethylaminopyran (or 3-ethoxy-2-dimethylaminopyran), which depends on the solvent and temperature.
3.  The equilibrium is shifted toward the 2H-pyran with increasing bulk of the solvent in the -position of the-dimethylaminodienone.
4.  The 2H-pyrans upon the action of UV light undergo reversible dissociation of the C-O bond and isomerize to-aminodienones.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1323–1335, June, 1989.  相似文献   

17.
1.  Absorption bands were observed in the UV spectra of saturated selenophosphoryl compounds that were attributed to the *, n *, and n - * transitions in the selenophosphoryl group.
2.  It was proposed to use the UV spectroscopy method to study the seleno-selenol isomerism in organophosphorus compounds.
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18.
1.  In the IR and Raman spectra of 3,3,6-trimethyl-6-hydroxy-7-chlorocyclohept-1-en-5-one when the phase and other conditions are varied there are indications of a conformational equilibrium involving at least three molecular forms.
2.  On the basis of this information as well as PMR spectra and examination of models it follows that in the liquid state the chair and twist boat forms occur. Similar results have also been obtained for 3,6-trimethyl-6-hydroxy-7-methoxycyclohept-1-en-5-one, in which hindered rotation about the C-OMe axis is also observed.
3.  Analysis of the spectra and models of 3,3,6-trimethyl-6,7-epoxycyclohept-1-en-5-ol and 3,3,6-trimethyl-6,7-epoxycyclohepten-5-one molecules has provided a conclusion about their possible conformations.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1555–1560, July, 1988.  相似文献   

19.
1.  Study has been made of the circular dichroism spectra of 20-ketosteroids containing a three-membered ring (methylene, epoxide, episulfide, or aziridine) in the -position with respect to the keto group.
2.  The observed n* and * transition Cotton effects have been correlated with the preferred conformation of the molecule.
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20.
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